EP1153997B1 - Adhésives thermofusibles - Google Patents

Adhésives thermofusibles Download PDF

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Publication number
EP1153997B1
EP1153997B1 EP01303794A EP01303794A EP1153997B1 EP 1153997 B1 EP1153997 B1 EP 1153997B1 EP 01303794 A EP01303794 A EP 01303794A EP 01303794 A EP01303794 A EP 01303794A EP 1153997 B1 EP1153997 B1 EP 1153997B1
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EP
European Patent Office
Prior art keywords
components
hot melt
melt adhesive
adhesive
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP01303794A
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German (de)
English (en)
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EP1153997A1 (fr
Inventor
Larry Frank Brinkman
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Rohm and Haas Co
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Rohm and Haas Co
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Publication of EP1153997A1 publication Critical patent/EP1153997A1/fr
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/36—Hydroxylated esters of higher fatty acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
    • C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
    • C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6212—Polymers of alkenylalcohols; Acetals thereof; Oxyalkylation products thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666—Compounds of group C08G18/48 or C08G18/52
    • C08G18/6696—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/36 or hydroxylated esters of higher fatty acids of C08G18/38
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
    • C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2170/00—Compositions for adhesives
    • C08G2170/20—Compositions for hot melt adhesives

Definitions

  • This invention relates to a hot melt adhesive composition, particularly a moisture reactive hot melt adhesive composition, a method for forming the adhesive composition, a method for bonding substrates, such as structural components, using the adhesive composition. More particularly this invention relates to a hot melt adhesive composition formed by admixing a polyisocyanate, an amorphous polyol, and 0.1 to 10%, by weight based on the weight of the adhesive composition, of certain styrene/allyl alcohol copolymers.
  • Hot melt adhesives are known to be desirable for their quick setting and for the absence of aqueous or solvent media which provide fluidity to other types of adhesives.
  • Moisture reactive hot melt adhesives which are based on an isocyanate group-containing urethane prepolymer can be designed to yield a relatively low melt viscosity for facile handling and application; reaction with moisture augments the final properties of the adhesive.
  • adhesive strength prior to completion of the reaction with moisture which is known in the art as "green strength” may be inadequate for necessary early handling of formed laminates.
  • low viscosity hot melt adhesives which via incorporation of crystalline polyesters or polyethers such as, for example, hexanediol adipates, polycaprolactones, and polytetramethyl ethylene glycol in the urethane prepolymers can crystallize during cooling after application to a substrate, thereby augmenting green strength.
  • crystalline polyesters or polyethers such as, for example, hexanediol adipates, polycaprolactones, and polytetramethyl ethylene glycol
  • many of the crystalline polyesters and polyethers are expensive and/or prone to hydrolytic attack over time.
  • U.S. Patent No. 4,999,407 discloses a quick-setting hot melt polyurethane composition which is a mixture of at least two amorphous polyurethane prepolymers, preferably a first polyurethane prepolymer having a Tg above room temperature and a second polyurethane prepolymer a Tg below room temperature
  • the problem faced by the inventor is the provision of an alternative moisture reactive hot melt adhesive composition containing a polyurethane prepolymer free from the reacted residues of crystalline polyester or polyether precursors and which provides effective bonding of substrates.
  • the inventor found that the incorporation of 0.1 to 10%, by weight based on the weight of the adhesive composition, of certain styrene/allyl alcohol addition copolymers into a polyurethane prepolymer-forming reaction mixture containing amorphous polyesters or polyethers and free from crystalline polyesters and polyethers provided the desired balance of properties.
  • a moisture reactive hot melt adhesive composition formed by admixing components including a polyisocyanate, an amorphous polyol, and 0.1 to 10%, by weight based on the weight of the adhesive composition, styrene/allyl alcohol copolymer having a hydroxyl number of 100-300 and Mn of 1,000-4,000, wherein the ratio of isocaynate groups/hydroxyl groups ("NCO/OH groups”) of the components on an equivalents basis is from 1.05 to 2.5, the components being free from crystalline polyesters and polyethers and the components containing less than 1%, by weight based on the total weight of the components, water.
  • a method for forming a moisture reactive hot melt adhesive by admixing components including a polyisocyanate, an amorphous polyol, and 0.1 to 10%, by weight based on the weight of the adhesive composition, styrene/allyl alcohol copolymer having a hydroxyl number of 100-300 and Mn of 1,000-4,000, wherein the ratio of NCO/OH groups of the components on an equivalents basis is from 1.05 to 2.5, the components being free from crystalline polyesters and polyethers and the components containing less than 1%, by weight based on the total weight of the components, water.
  • a method for bonding substrates by forming a moisture reactive hot melt adhesive including admixing components including a polyisocyanate, an amorphous polyol, and 0.1 to 10%, by weight based on the weight of the adhesive composition, styrene/allyl alcohol copolymer having a hydroxyl number of 100-300 and Mn of 1,000-4,000, wherein the ratio of NCO/OH groups of the components on an equivalents basis is from 1.05 to 2.5, the components being free from crystalline polyesters and polyethers and the components containing less than 1%, by weight based on the total weight of the components, water; heating the adhesive to a temperature of 50 °C to 160 °C; applying the heated hot melt adhesive to a first substrate in the presence of moisture; contacting the applied heated hot melt adhesive with a second substrate; and cooling, or allowing to cool, the adhesive.
  • components including a polyisocyanate, an amorphous polyol, and 0.1 to 10%, by weight based on the weight of the adhesive composition
  • the composition of this invention is a moisture reactive hot melt adhesive composition.
  • moisture reactive is meant herein that the composition contains isocyanate groups which are capable of reacting with water desirably to effect an increase in the molecular weight of the adhesive composition and/or effect crosslinking of the adhesive composition so as to increase the strength properties of the adhesive subsequent to being contacted with water.
  • hot melt is meant herein that the adhesive which may be a solid, semi-solid or viscous mass can be advantageously heated to provide a fluid adhesive of a viscosity suitable for application to and adhesion to substrates.
  • the moisture reactive hot melt adhesive composition of the present invention is formed by admixing components which include a polyisocyanate, i.e., an isocyanate bearing at least two isocyanate groups.
  • Polyisocyanates which may be used include aromatic, aliphatic, cycloaliphatic polyisocyanates and combinations thereof, such as, for example, m-phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, hexamethylene diisocyanate, tetramethylene diisocyanate, 1,4-cyclohexane diisocyanate, hexahydrotoluene diisocyanate, 1,5-naphthalene diisocyanate, 1-methoxy-2,4-phenylene diisocyanate, 4,4'-diphenylmethane diisocyanate, 2,4-diphenylmethane diisocyanate, 4,4'-bi
  • the moisture reactive hot melt adhesive composition of the present invention is formed by admixing components which include an amorphous polyol, by which is meant a polyol bearing two or more hydroxyl groups, which polyol does not crystallize under ambient conditions.
  • amorphous polyols such as amorphous polyesters and amorphous polyethers, polyester/polyethers having both ester and ether linkages, and mixtures thereof may be used.
  • the amorphous polyols preferably have a weight average molecular weight ("Mw") as measured by gel permeation chromatograph, from 250 to 8,000, more preferably from 250 to 3,000 and preferably have an acid number less than 5, more preferably less than 2.
  • Amorphous polyester polyols are preferably aromatic such as those formed from phthalic anhydride and diethylene glycol.
  • Amorphous polyether polyols may be prepared by the reaction of an alkylene oxide with a polyhydric alcohol.
  • the moisture reactive hot melt adhesive composition of the present invention is formed by admixing components which include 0.1 to 10%, by weight based on the weight of the polyol, of a styrene/allyl alcohol addition copolymer having a hydroxyl number of 100-300 and Mn of 1,000-4,000.
  • a styrene/allyl alcohol addition copolymer having a hydroxyl number of 100-300 and Mn of 1,000-4,000.
  • Such copolymers are commercially available from Lyondell Chemical, Houston, Texas such as SAA-100, disclosed to be 70 styrene/30 allyl alcohol, on a molar basis, and SAA-103, disclosed to be 80 styrene/20 allyl alcohol, on a molar basis.
  • styrene/allyl alcohol addition copolymer herein is mean a copolymer containing at least 90 weight percent of copolymerized residues of styrene and allyl alcohol but not excluding other copolymerized monomer(s) to an extent of less than 10 weight percent based on the weight of the copolymer. Without being bound by mechanism, it is believed that the styrene/allyl alcohol copolymer which has, at ambient temperature, crystalline properties, may induce sufficient ordering in the adhesive composition into which it is incorporated to effect a useful level of green strength prior to the reaction of the adhesive with moisture.
  • copolymer compositions having a hydroxyl number of 100-300 and Mn of 1,000-4,000 and exhibiting crystalline properties at ambient temperature will also be useful in the moisture reactive hot melt adhesive composition and method for bonding substrates of this invention.
  • the ratio of NCO/OH groups from all of the admixed components taken on an equivalents basis is from 1.05 to 2.5, preferably from 1.1 to 2.0 in order to provide an adhesive composition with an excess of isocyanate groups.
  • the components are free from crystalline polyesters and polyethers.
  • the components contain less than 1% water, preferably less than 0.2% water, by weight based on the total weight of the components.
  • the components are mixed by conventional means, preferably in an inert, dry atmosphere, and reacted, preferably at a temperature of 50 °C to 120 °C., preferably for a time sufficient to achieve a hydroxyl number of less than 25, more preferably for a time sufficient to achieve a hydroxyl number of less than 5.
  • the styrene/allyl alcohol addition copolymer is preferably solubilized by heating and mixing with at least one of the non-isocyanate containing components before the reaction with the polyisocyanate.
  • a catalyst such as, for example, a tertiary amine or a tin-based catalyst may be admixed with the components at a level of less than 0.3% by weight based on the total weight of the admixed components, either before, during, or after the reaction to form the adhesive composition.
  • the adhesive composition of this invention which is a NCO-functional adhesive, is stored, preferably under an inert, dry atmosphere until use.
  • the hot melt adhesive composition may be formulated by admixing additional conventional ingredients such as fillers, pigments, tackifiers, plasticizers, rheology modifiers, thermoplastic acrylic resins, etc. with due regard to the reactivity of the NCO-functional groups which are desirably maintained.
  • the moisture reactive hot melt adhesive is heated to a temperature of 50-160 °C, preferably to a temperature of 100 °C to 150 °C, in order to achieve a viscosity suitable for transporting the adhesive, such as by pumping or gravity feed, to the application equipment and for the application of the adhesive to a first substrate in the presence of moisture.
  • the application of the adhesive may be effected by conventional means such as, for example, heated spray applicator, heated bead applicator, heated nozzle, and heated roll coater, to form a continuous or discontinuous film of adhesive, as desired.
  • the adhesive may typically be applied at a level of 3.7 to 18.6 kg/sq.
  • the moisture i.e., water
  • the moisture may be, for example, a result of ambient humidity, artificially increased or controlled humidified air, a mist of water droplets, or a spray of liquid water contacting the applied adhesive.
  • the moisture may be augmented by other NCO-functional group-reactive ingredients such as, for example, amines.
  • the applied adhesive is contacted by a second substrate to provide a laminate construction.
  • the laminate construction so formed is optionally subjected to applied pressure such as by passing it between rollers to effect increased contact of the substrates with the adhesive and the laminate construction is then cooled or allowed to cool.
  • the adhesive may be simultaneously or sequentially applied to both surfaces of the first substrate which adhesive are then simultaneously or sequentially bonded to two further substrates, which may be the same or different. It is further contemplated that the laminate construction may subsequently be bonded to other substrate(s) using the same or a different adhesive before or after the process described herein.
  • the first and second substrates to be bonded in the method of this invention may be the same or different and include, for example, metal, wood, consolidated wood products, paper, woven and nonwoven fabrics, and plastics which may have smooth or structured surfaces and are provided in the form of rolls, sheets, films, foils, etc. They include, for example, lauan mahogany plywood, impregnated paper, extruded polstyrene foam, expanded polystyrene foam, fiberglass reinforced polyester, polyester fabric, high or low pressure laminate, plywood, aluminum, steel, PVC, and engineering plastics.
  • a one liter reaction vessel was set up with, a gas inlet tube, thermometer, stirrer and a heating jacket.
  • the cured free film of the product had the following properties: ( after 7days at 21.1 °C (70 °F), 50 % Relative Humidity ) 10.91 MPa (1583 psi) tensile strength 599 % elongation 1.5 MPa (219 psi) modulus
  • a hot melt adhesive was prepared according to the process of Example 1 with materials as presented below.
  • a hot melt adhesive was prepared according to the process of Example 1 with materials as presented below. with the addition of a non-reactive, thermoplastic, styrene/ ⁇ - methyl styrene resin reinforcing resin. The resin was added with the initial charge materials and brought into solution with heat and stirring as in Example 1.
  • a hot melt adhesive was prepared according to the process of Example 3 with the addition of an additional hydroxyl polymer which was added with the inital charge.
  • a hot melt adhesive was prepared according to the process of Example 2 with higher molecular weight polypropylene glycol.
  • a 1.22 meter (four foot) wide hot melt roll coater with an upper and lower set of rolls was allowed to preheat to 126.7 °C (260 °F).
  • a doctor roll was used to adjust the coating thickness by adjusting the gap between the doctor roll and the applicator roll.
  • Spring-loaded end seals contacted the ends of both doctor and applicator rolls to form a well for the adhesive. This set of rolls was then lowered to contact the substrate to be coated.
  • the lower applicator roll contacted the bottom of the substrate.
  • When power was supplied to the rolls they pulled the first substrate through and coated it.
  • a second substrate was placed on the adhesive by hand and the laminate was run through a rotary press which forced the adhesive into positive contact with the second substrate.
  • the laminate was set aside to moisture cure. Green strength was tested by observing lifting or pulling apart of the substrates (due to memory or warp or twisting when the laminate was moved).
  • the hot melt adhesive of Example 1 was applied to a series of first substrates at 123 - 129 g/sqm. (11.5-12 g/sq ft.) except for textured aluminium where adhesive was applied at a level of 161 g/sq.m. (15 g/sq ft.), and then contacted with a second substrate as described above to form laminates. 7.62 cm. (3 inch) strips of the laminates were peeled back by hand after 24 or 48 hours at 21.1 °C (70 °F) and 50 % Relative Humidity.
  • FRP and lauan were bonded with the adhesive composition of Example 1 according to the method of Example 7.
  • Tensile shear and flatwise. tensile after aging for 7 days at 21.1 °C (70 °F) and 50 % Relative Humidity are presented in Tables 8.1 and 8.2 below.
  • Tensile shear data Temperature Average Tensile Shear (psi) Type of Failure 23.9 °C (75 °F) 1.77 MPa (256) Lauan failure 48.9 °C (120 °F) 3.49 MPa (500) Lauan failure 71.1 °C (160 °F) 2.84 MPa (412) Adhesive failure Flatwise tensile data Temperature Average tensile (psi) 71.1 °C (160 °F) 0.807 MPa 117 82.2 °C (180 °F) 0.58 MPa 84

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Polyurethanes Or Polyureas (AREA)

Claims (3)

  1. Composition adhésive thermofusible réagissant à l'humidité, formée par mélange de composants comprenant un polyisocyanate, un polyol amorphe et de 0,1 à 10 % en poids par rapport au poids de ladite composition adhésive d'un copolymère styrène/alcool allylique ayant un indice d'hydroxyle de 100 à 300 et une Mn de 1 000 à 4 000, où le rapport des groupes NCO/OH desdits composants, sur une base en équivalents, est de 1,05 à 2,5, lesdits composants étant exempts de polyesters et de polyéthers cristallins, et lesdits composants contenant moins de 1 % en poids d'eau par rapport au poids total desdits composants.
  2. Procédé pour former un adhésif thermofusible réagissant à l'humidité, qui comprend le mélange de composants comprenant un polyisocyanate, un polyol amorphe et de 0,1 à 10 % en poids par rapport au poids de ladite composition adhésive d'un copolymère styrène/alcool allylique ayant un indice d'hydroxyle de 100 à 300 et une Mn de 1 000 à 4 000, où le rapport des groupes NCO/OH desdits composants, sur une base en équivalents, est de 1,05 à 2,5, lesdits composants étant exempts de polyesters et de polyéthers cristallins, et lesdits composants contenant moins de 1 % en poids d'eau par rapport au poids total desdits composants.
  3. Procédé pour relier des substrats, qui consiste
       à former un adhésif thermofusible réagissant à l'humidité, en mélangeant des composants comprenant un polyisocyanate, un polyol amorphe et de 0,1 à 10 % en poids par rapport au poids de ladite composition adhésive d'un copolymère styrène/alcool allylique ayant un indice d'hydroxyle de 100 à 300 et une Mn de 1 000 à 4 000, où le rapport des groupes NCO/OH desdits composants, sur une base en équivalents, est de 1,05 à 2,5, lesdits composants étant exempts de polyesters et de polyéthers cristallins, et lesdits composants contenant moins de 1 % en poids d'eau par rapport au poids total desdits composants ;
       à chauffer ledit adhésif à une température de 50 à 160°C ;
       à appliquer ledit adhésif thermofusible chauffé sur un premier substrat en présence d'humidité ;
       à mettre en contact avec un deuxième substrat ledit adhésif thermofusible chauffé appliqué ; et
       à refroidir ou à laisser refroidir ledit adhésif.
EP01303794A 2000-05-10 2001-04-26 Adhésives thermofusibles Expired - Lifetime EP1153997B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US20330300P 2000-05-10 2000-05-10
US203303P 2000-05-10

Publications (2)

Publication Number Publication Date
EP1153997A1 EP1153997A1 (fr) 2001-11-14
EP1153997B1 true EP1153997B1 (fr) 2003-06-25

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Country Status (9)

Country Link
US (1) US6579406B2 (fr)
EP (1) EP1153997B1 (fr)
JP (1) JP3932015B2 (fr)
CN (1) CN1256384C (fr)
AU (1) AU3896501A (fr)
BR (1) BR0101815A (fr)
DE (1) DE60100395T2 (fr)
MX (1) MXPA01004449A (fr)
TW (1) TW555821B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101585277B1 (ko) 2007-12-20 2016-01-13 헨켈 아게 운트 코. 카게아아 섬유상 주형부를 접착하기 위한 2 성분 폴리우레탄 접착제

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US6911491B2 (en) * 2001-04-20 2005-06-28 Rohm And Haas Company Hot melt adhesive
MXPA02011491A (es) * 2001-12-06 2003-06-30 Rohm & Haas Adhesivo de fusion en caliente.
TW200305587A (en) * 2002-03-19 2003-11-01 Rohm & Haas Urethane polymer compositions
US7098291B2 (en) 2002-06-10 2006-08-29 Rohm And Haas Company Urethane polymer compositions
DE102004035764A1 (de) * 2004-07-23 2006-03-16 Bayer Materialscience Ag Niedrigviskose Polyurethan-Prepolymere auf Basis von 2,4'-MDI
DE102005052813A1 (de) * 2005-11-05 2007-05-10 Bayer Materialscience Ag MDI-Prepolymere und darauf basierende Lacke mit verbesserten Eigenschaften, ein Verfahren zu ihrer Herstellung und ihre Verwendung
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AU3896501A (en) 2001-11-15
DE60100395D1 (de) 2003-07-31
CN1256384C (zh) 2006-05-17
BR0101815A (pt) 2001-12-18
US6579406B2 (en) 2003-06-17
CN1322790A (zh) 2001-11-21
DE60100395T2 (de) 2004-04-22
EP1153997A1 (fr) 2001-11-14
JP3932015B2 (ja) 2007-06-20
JP2001316654A (ja) 2001-11-16
TW555821B (en) 2003-10-01
US20020033228A1 (en) 2002-03-21

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